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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Membrane model as key tool in the study of glutathione-s-transferase mediated anticancer drug resistance

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Author(s):
Materon, Elsa M. [1, 2] ; Shimizu, Flavio M. [1, 3] ; dos Santos, Kevin Figueiredo [1] ; Nascimento, Gustavo F. [1] ; Geraldo, Vananelia P. N. [1] ; Oliveira Jr, Osvaldo N. ; Faria, Ronaldo C. [2]
Total Authors: 7
Affiliation:
[1] Univ Sao Paulo, Sao Carlos Inst Phys, POB 369, BR-13560970 Sao Carlos, SP - Brazil
[2] Univ Fed Sao Carlos, Chem Dept, CP 676, BR-13565905 Sao Carlos, SP - Brazil
[3] Univ Estadual Campinas, Gleb Wataghin Inst Phys IFGW, Dept Appl Phys, UNICAMP, BR-13083859 Campinas, SP - Brazil
Total Affiliations: 3
Document type: Journal article
Source: BIOMEDICINE & PHARMACOTHERAPY; v. 145, JAN 2022.
Web of Science Citations: 0
Abstract

Glutathione-s-transferase is believed to be involved in the resistance to chemotherapeutic drugs, which depends on the interaction with the cell membranes. In this study, we employed Langmuir monolayers of a mixture of phospholipids and cholesterol (MIX) as models for tumor cell membranes and investigated their interaction with the anticancer drugs cisplatin (CDDP) and doxorubicin (DOX). We found that both DOX and CDDP expand and affect the elasticity of MIX monolayers, but these effects are hindered when glutathione-s-transferase (GST) and its cofactor glutathione (GSH) are incorporated. Changes are induced by DOX or CDDP on the polarizationmodulated infrared reflection absorption spectroscopy (PM-IRRAS) data for MIX/GST/GSH monolayers, thus denoting some degree of interaction that is not sufficient to alter the monolayer mechanical properties. Overall, the results presented here give support to the hypothesis of the inactivation of DOX and CDDP by GST and point to possible directions to detect and fight drug resistance. (AU)

FAPESP's process: 12/15543-7 - Biosensors to detect Escherichia coli using the concept of an extended electronic tongue
Grantee:Flavio Makoto Shimizu
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 17/24053-7 - Development of simple electrochemical methods for the detection of biomarkers for the diagnosis of diseases
Grantee:Ronaldo Censi Faria
Support Opportunities: Regular Research Grants
FAPESP's process: 16/00991-5 - Study of Detoxification Enzymes Interaction with chemotherapeutic drugs and its relationship with chemoresistance
Grantee:Elsa María Materón Vásques
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 18/22214-6 - Towards a convergence of technologies: from sensing and biosensing to information visualization and machine learning for data analysis in clinical diagnosis
Grantee:Osvaldo Novais de Oliveira Junior
Support Opportunities: Research Projects - Thematic Grants